Novel synthesis of O6-alkylguanine containing oligodeoxyribonucleotides as substrates for the human DNA repair protein, O6-methylguanine DNA methyltransferase (MGMT)

Nucleic Acids Res. 2006 Apr 11;34(6):1884-91. doi: 10.1093/nar/gkl117. Print 2006.

Abstract

The human DNA repair protein O6-methylguanine DNA methyltransferase (MGMT) dealkylates mutagenic O6-alkylguanine lesions within DNA in an irreversible reaction which results in inactivation of the protein. MGMT also provides resistance of tumours to alkylating agents used in cancer chemotherapy and its inactivation is therefore of particular clinical importance. We describe a post-DNA synthesis strategy which exploits the novel, modified base 2-amino-6-methylsulfonylpurine and allows access for the first time to a wide variety of oligodeoxyribonucleotides (ODNs) containing O6-alkylguanines. One such ODN containing O6-(4-bromothenyl)guanine is the most potent inactivator described to date with an IC50 of 0.1 nM.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Guanine / analogs & derivatives*
  • Guanine / chemistry
  • Humans
  • O(6)-Methylguanine-DNA Methyltransferase / metabolism*
  • Oligodeoxyribonucleotides / chemical synthesis*
  • Oligodeoxyribonucleotides / chemistry
  • Oligodeoxyribonucleotides / metabolism
  • Organophosphorus Compounds / chemical synthesis
  • Organophosphorus Compounds / chemistry

Substances

  • O(6)-(4-bromothenyl)guanine
  • Oligodeoxyribonucleotides
  • Organophosphorus Compounds
  • phosphoramidite
  • Guanine
  • O(6)-Methylguanine-DNA Methyltransferase